Aggressive orbital rhabdomyosarcoma in adulthood: A case report in a public hospital in Damascus, Syria

Orbital rhabdomyosarcoma (RMS) is a highly malignant tumor that originates mainly from mesenchymal tissue. It is considered a rare childhood malignancy; therefore, presentation in adulthood is scarce. In this case report, a 36-year-old male patient presented with a rapidly progressive RMS of the lef...

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Autores principales: Tagrid Younes Ahmad, Hasan Nabil Al Houri, Abdullah Nabil Al Houri, Nagham Younes Ahmad
Formato: article
Lenguaje:EN
Publicado: Thieme Medical and Scientific Publishers Pvt. Ltd. 2018
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Acceso en línea:https://doaj.org/article/6ae093a9272f413bae66f433c7be28a5
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